医学
化疗
内科学
肺癌
放射治疗
耐火材料(行星科学)
疾病
靶向治疗
血液学
癌症研究
癌症
肿瘤科
生物
天体生物学
作者
Dwight Hall Owen,Michael J. Giffin,Julie M. Bailis,Marie-Anne Damiette Smit,David Paul Carbone,Kai He
标识
DOI:10.1186/s13045-019-0745-2
摘要
Small cell lung cancer (SCLC) accounts for approximately 15% of all lung cancers. Despite high rates of response to first-line chemotherapy and radiotherapy, patients with extensive-stage disease eventually relapse, and very few patients survive more than 5 years from diagnosis. Treatment options for recurrent or refractory disease are limited, and the treatments that do exist are associated with significant treatment-related toxicities. Delta-like ligand 3 (DLL3) is an inhibitory Notch ligand that is highly expressed in SCLC and other neuroendocrine tumors but minimally expressed in normal tissues. It is therefore being explored as a potential therapeutic target in SCLC. Here, we review the preclinical and clinical evidence for targeting DLL3 in SCLC and discuss several DLL3-specific therapies being developed for the treatment of SCLC: the antibody-drug conjugate rovalpituzumab tesirine, the bispecific T cell engager immuno-oncology therapy AMG 757, and the chimeric antigen receptor T cell therapy AMG 119.
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